search
Back to results

Betaglucin 0.2% Versus Imiquimod 5% in Treatment of Ano-genital Warts: Combined Results From Triple Blind Controlled Study (BETAGENWART)

Primary Purpose

Genital Wart Virus Infection

Status
Unknown status
Phase
Phase 3
Locations
Nicaragua
Study Type
Interventional
Intervention
Betaglucin soluble gel 0.2%
Imiquimod 5% cream
Sponsored by
Centro de Investigaciones Medicas y Ensayos Clinicos Dr Italo Fabbri
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Genital Wart Virus Infection focused on measuring Betaglucin soluble gel, Ano-genital warts, Clearance, Human papillomavirus

Eligibility Criteria

18 Years - 50 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Men and women aged 18 to 50 years with anogenital wart visible on physical examination and positive for HPV 6 and 11 by polymerase chain reaction (PCR) test with detection by agarose gel electrophoresis.

Exclusion Criteria:

  • Pregnant women.
  • Vaccinated against human papillomavirus (Gardasil, Gardasil 9 or Cervarix).
  • Patients Immunosuppressed by drugs (Chemotherapy, Corticoids, use of antibiotics for more than 7 days and/or antituberculous treatment.)
  • Molluscum contagiosum.
  • Skin Appendages.
  • Urethral prolapse.
  • Botryoid sarcoma.
  • Herpes type II.
  • History of anogenital surgery in the last 4 weeks.
  • Intake of natural products or immunomodulators.
  • Patients who have received 5% imiquimod cream.

Sites / Locations

  • Clínica San DominicRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Arm Betaglucin

Arm Imiquimod

Arm Description

It will be composed of 51 individuals between 18 and 50 years old with anogenital warts to which will be applied betaglucin gel at 0.2%.

51 individuals between the ages of 18 and 50 will receive 5% imiquimod.

Outcomes

Primary Outcome Measures

Cure Rate
Completely cured will be those that present a disappearance of 80% or more of the initial volume of the wart, partially cured will be a decrease of at least 50%-79% of the initial volume of the lesion using a measurement rule applied to the larger diameter of this and not cured those that present a reduction of less than 50% of the initial volume.

Secondary Outcome Measures

Full Information

First Posted
March 28, 2019
Last Updated
February 3, 2020
Sponsor
Centro de Investigaciones Medicas y Ensayos Clinicos Dr Italo Fabbri
Collaborators
CALOX Laboratories, Bioanalisis
search

1. Study Identification

Unique Protocol Identification Number
NCT03901690
Brief Title
Betaglucin 0.2% Versus Imiquimod 5% in Treatment of Ano-genital Warts: Combined Results From Triple Blind Controlled Study
Acronym
BETAGENWART
Official Title
Betaglucin 0.2% Gel Versus Imiquimod Cream 5% in the Treatment of Anogenital Warts in 102 Individuals Older Than 18 Years.
Study Type
Interventional

2. Study Status

Record Verification Date
February 2020
Overall Recruitment Status
Unknown status
Study Start Date
August 27, 2019 (Actual)
Primary Completion Date
March 10, 2020 (Anticipated)
Study Completion Date
May 20, 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Centro de Investigaciones Medicas y Ensayos Clinicos Dr Italo Fabbri
Collaborators
CALOX Laboratories, Bioanalisis

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
In order to determine the Efficacy of Betaglucin 0.2% in gel vs Imiquimod 5% cream in the treatment of 102 individuals older than 18 years with anogenital warts trials in two arms 51 with Betaglucin 0.2% and 51 with Imiquimod 5%.
Detailed Description
Betaglucin soluble gel at 0.2% is produced in Costa Rica by a biochemical researcher. Obtained by chemical process improves the immune response by increasing 80 times the number of macrophages and Natural Killer cells. Specifically in human papillomavirus-related anogenital warts. As clinical researchers, the investigators pretend to determine the therapeutic efficacy of betaglucin 0.2 % gel compared with Imiquimod 5% cream in two groups of individuals from 18 to 50 years old males and females. Based in mathematics and biostatistics formula used by Professor Roman Fentin, French academic working in the University of Costa Rica. Medicine Faculty in San Jose the number of participants should be 102. Divided into two arms. Arm betaglucin 0.2% 51 individuals treated with betaglucin soluble gel at 0.2% Arm imiquimod 5% 51 individuals treated with imiquimod cream at 5 % After three months of follow-up of all individuals, will be classified as clearance, partially cured and not cured. The plan of analysis will be: Chi-square test between the two groups (depending on the treatment) and the success or not of the treatment. Logistic model with a dependent variable the success or not of the treatment and with independent variables the treatment, sex, age. It will make it possible to verify that the differences observed in 1 are not due to another factor. Logistic model with a dependent variable the success or not of the treatment and with independent variables the treatment, the sex, the age, and an interaction sex-age. It will allow us to observe if there is a difference in the result according to the patient's sex.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Genital Wart Virus Infection
Keywords
Betaglucin soluble gel, Ano-genital warts, Clearance, Human papillomavirus

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Model Description
prospective triple-blind randomized controlled clinical trial
Masking
ParticipantInvestigatorOutcomes Assessor
Masking Description
In this clinical trial, the masking is triple because neither the participants nor the researchers nor the outcomes assessor will know exactly which drug will receive. Only through a list created mathematically by Prof R Fentin will serve as a unique guide for the administration masked either beta-glucan gel or imiquimod in cream. Both packaged in the same tube without labeling on the outside.
Allocation
Randomized
Enrollment
102 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Arm Betaglucin
Arm Type
Experimental
Arm Description
It will be composed of 51 individuals between 18 and 50 years old with anogenital warts to which will be applied betaglucin gel at 0.2%.
Arm Title
Arm Imiquimod
Arm Type
Active Comparator
Arm Description
51 individuals between the ages of 18 and 50 will receive 5% imiquimod.
Intervention Type
Drug
Intervention Name(s)
Betaglucin soluble gel 0.2%
Intervention Description
With the prior informed consent of the 51 study participants, 5 grams of 0.2% soluble betaglucin gel will be self-applied every 12 hours for 5 days. Both groups will receive an unlabeled tube so that none of the study participants will know what topical treatments they are receiving.
Intervention Type
Drug
Intervention Name(s)
Imiquimod 5% cream
Intervention Description
With the prior informed consent of the 51 study participants, 1 gram of 5% imiquimod will be self-applied once a day for 5 days. Both groups will receive an unlabeled tube so that neither study participant knows what topical treatments they are receiving.
Primary Outcome Measure Information:
Title
Cure Rate
Description
Completely cured will be those that present a disappearance of 80% or more of the initial volume of the wart, partially cured will be a decrease of at least 50%-79% of the initial volume of the lesion using a measurement rule applied to the larger diameter of this and not cured those that present a reduction of less than 50% of the initial volume.
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Men and women aged 18 to 50 years with anogenital wart visible on physical examination and positive for HPV 6 and 11 by polymerase chain reaction (PCR) test with detection by agarose gel electrophoresis. Exclusion Criteria: Pregnant women. Vaccinated against human papillomavirus (Gardasil, Gardasil 9 or Cervarix). Patients Immunosuppressed by drugs (Chemotherapy, Corticoids, use of antibiotics for more than 7 days and/or antituberculous treatment.) Molluscum contagiosum. Skin Appendages. Urethral prolapse. Botryoid sarcoma. Herpes type II. History of anogenital surgery in the last 4 weeks. Intake of natural products or immunomodulators. Patients who have received 5% imiquimod cream.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Alejandro Perez Fabbri, OBGYN
Phone
+505 8626-1994
Email
cimif.director.ejecutivo@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Hellen Guevara, MSC
Phone
+505 89988021
Email
cimif.secretaria.ejecutiva@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Romain Fantin, PhD. Math
Organizational Affiliation
Centro de Investigaciones Medicas y Ensayos Clinicos Dr Italo Fabbri
Official's Role
Study Chair
Facility Information:
Facility Name
Clínica San Dominic
City
Managua
ZIP/Postal Code
14027
Country
Nicaragua
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Alejandro P Perez Fabbri, FACOG ObGyn
Phone
505 86261994
Email
medicoenconsulta27@gmail.com
First Name & Middle Initial & Last Name & Degree
Helen C Guevara, MSC
Phone
505 8998 8021
Email
guevarad1@yahoo.com

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
There is a timeline that includes a start date, end date, informed consent signature, study protocol, statistical analysis plan, informed consent form, clinical study report.
IPD Sharing Time Frame
Available on May 2019 until May 2021
IPD Sharing Access Criteria
Available for clinical researchers, professors and health care providers
IPD Sharing URL
http://cimif.org
Citations:
PubMed Identifier
21876641
Citation
Baker DA, Ferris DG, Martens MG, Fife KH, Tyring SK, Edwards L, Nelson A, Ault K, Trofatter KF, Liu T, Levy S, Wu J. Imiquimod 3.75% cream applied daily to treat anogenital warts: combined results from women in two randomized, placebo-controlled studies. Infect Dis Obstet Gynecol. 2011;2011:806105. doi: 10.1155/2011/806105. Epub 2011 Aug 24.
Results Reference
background
PubMed Identifier
20938424
Citation
Scardamaglia P, Carraro C, Mancino P, Stentella P. [Effectiveness of the treatment with beta-glucan in the HPV-CIN 1 lesions]. Minerva Ginecol. 2010 Oct;62(5):389-93. Italian.
Results Reference
result

Learn more about this trial

Betaglucin 0.2% Versus Imiquimod 5% in Treatment of Ano-genital Warts: Combined Results From Triple Blind Controlled Study

We'll reach out to this number within 24 hrs